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Chemical Structure| 1198437-43-2 Chemical Structure| 1198437-43-2

Structure of 1198437-43-2

Chemical Structure| 1198437-43-2

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Product Details of [ 1198437-43-2 ]

CAS No. :1198437-43-2
Formula : C8H11FN2O2
M.W : 186.18
SMILES Code : O=C(C1=NN(CCF)C=C1)OCC
MDL No. :MFCD26386313

Safety of [ 1198437-43-2 ]

Application In Synthesis of [ 1198437-43-2 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1198437-43-2 ]

[ 1198437-43-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 762-51-6 ]
  • [ 5932-27-4 ]
  • [ 1198437-43-2 ]
  • [ 1198437-41-0 ]
YieldReaction ConditionsOperation in experiment
Intermediates 72 and 73Ethyl 1-(2-fluoroethyl)-1H-pyrazole-5-carboxylate and ethyl 1-(2-fluoroethyl)-1H- pyrazole-3-carboxylate To a solution of ethyl 1 H-pyrazole-3-carboxylate (0.77g) (available from ABCR) in acetonitrile (30ml) was added cesium carbonate (1.79g) and the mixture stirred for 5min when 1-fluoro-2-iodoethane (0.96g) was added and the mixture stirred at 200C for 18h.The mixture was evaporated and the residue taken up in water (30ml) and DCM (30ml) separated by hydrophobic frit and concentrated to ~5ml, placed on an SPE cartridge (5Og silica) and eluted with a gradient of ethyl acetate in cyclohexane to give the Ethyl 1-(2- fluoroethyl)-1 H-pyrazole-5-carboxylate (0.42g) as a colourless oil.LC/MS R1 2.09 min m/z 186 [MH+]. Method C and ethyl 1-(2-fluoroethyl)-1 H-pyrazole-3-carboxylate (g) as a colourless oilLC/MS R1 1.73 min m/z 186 [MH+]. Method C
  • 2
  • [ 762-49-2 ]
  • [ 5932-27-4 ]
  • [ 1198437-43-2 ]
YieldReaction ConditionsOperation in experiment
47% To a suspension of <strong>[5932-27-4]1H-<strong>[5932-27-4]pyrazole-3-carboxylic acid ethyl ester</strong></strong> (12.0 g, 85.67 mmol) in THF (250 mL) at 0 C. was added NaH (3.08 g, 128.51 mmol) in small portions. The mixture was stirred for 30 min. Then 2-fluoro-1-bromo ethane (11.87 g, 94.24 mmol) was added. The temperature was slowly increased to 80 C. and the mixture was left with stirring overnight. The mixture was quenched with ice-cold water and extracted with EtOAc (2*150 mL). The combined organic layers were dried over Na2SO4 and evaporated to dryness. Flash chromatography (silica, EtOAc:petroleum ether 3:7) gave 1-(2-fluoro-ethyl)-<strong>[5932-27-4]1H-<strong>[5932-27-4]pyrazole-3-carboxylic acid ethyl ester</strong></strong> as an off-white solid (7.5 g, 47%).
With potassium carbonate; sodium iodide; In N,N-dimethyl-formamide; at 100℃; for 48h;Sealed tube; Step 1:; To a solution of 1 H-<strong>[5932-27-4]pyrazole-3-carboxylic acid ethyl ester</strong> S (500 mg, 3.57 mmol) in DMF (6.5 mL) is added K2C03 (542 mg, 3.93 mmol, 1.10 equiv), Nal (1.07 g, 7.14 mmol, 2 equiv) and 1-bromo-2-fluoroethane (928 mg, 7.14 mmol, 2.00 equiv). The reaction mixture is stirred at 100 C for 48 h in a closed vial. The reaction is quenched with HCI 1 N (pH ~5-6), water is added and the mixture is extracted with EtOAc (5x). The organics are washed with brine, dried with anhydrous MgS04, filtered and concentrated. The crude mixture containing the 2 regioisomers is purified by prep HPLC. The appropriate fractions are combined, frozen and lyophilized to give Td.UPLC-MS: 186.8 (M+H)+ 1H NMR (400 MHz, DMSO-d6) delta (ppm): 7.90 (d, J = 2.4 Hz, 1 H), 6.76 (d, J = 2.4 Hz, 1 H), 4.79 (dt, J = 47.3, 4.7 Hz, 2H), 4.53 (dt, J = 27.8, 4.7 Hz, 2H), 4.26 (q, J = 7.1 Hz, 2H), 1.28 (t, J = 7.1 Hz, 3H).
With potassium carbonate; sodium iodide; In N,N-dimethyl-formamide; at 100℃; for 48h; Step 1:; To a solution of 1 H-<strong>[5932-27-4]pyrazole-3-carboxylic acid ethyl ester</strong> 9a (500 mg, 3.57 mmol) in DMF (6.5 mL) is added K2C03 (542 mg, 3.93 mmol, 1 .10 equiv), Nal (1 .07 g, 7.14 mmol, 2.00 equiv) and 1 -bromo-2-fluoroethane (928 mg, 7.14 mmol, 2.00 equiv). The reaction mixture is stirred at 100 C for 48 h in a closed vial. The reaction is quenched with HCI 1 N (pH ~5-6), water is added and the mixture is extracted with EtOAc (5x). The organics are washed with brine, dried with anhydrous MgS04, filtered and concentrated. The crude mixture containing the 2 regioisomers is purified by prep HPLC. The appropriate fractions are combined, frozen and lyophilized to give 9g.UPLC-MS: 186.8 (M+H)+ 1H NMR (400 MHz, DMSO-d6) delta (ppm): 7.90 (d, 1 H, J = 2.4 Hz), 6.76 (d, 1 H, J = 2.4 Hz), 4.79 (dt, 2H, J = 47.3, 4.7 Hz), 4.53 (dt, 2H, J = 27.8, 4.7 Hz), 4.26 (q, 2H, J = 7.1 Hz), 1 .28 (t, 3H, J = 7.1 Hz).
 

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